Zhang Qingguo, Gong Weiming, Ning Bin, Nie Lin, Wooley Paul H, Yang Shang-You
Orthopaedic Research Institute, Via Christi Wichita Hospitals, Wichita, KS 67214, USA ; Jinan Central Hospital, Shandong University, Jinan 250013, China.
ScientificWorldJournal. 2013 Oct 3;2013:718061. doi: 10.1155/2013/718061. eCollection 2013.
This study examined the influence of osteoprotegerin (OPG) gene transfer on a murine collagen-induced arthritis model. A single periarticular injection of AAV-OPG or AAV-LacZ on the arthritic paw successfully incorporated the exogenous gene to the local tissue and resulted in marked transgene expression in the joint homogenate for at least three weeks. Clinical disease scores were significantly improved in OPG treated mice starting at 28-day post-treatment (P < 0.05). Histological assessment demonstrated that OPG gene transfer dramatically protected mice from erosive joint changes compared with LacZ controls (P < 0.05), although treatment appeared less effective on the local inflammatory progress. MicroCT data suggested significant protection against subchondral bone mineral density changes in OPG treated CIA mice. Interestingly, mRNA expressions of IFN-g and MMP3 were noticeably diminished following OPG gene transfer. Overall, gene transfer of OPG effectively inhibited the arthritis-associated periarticular bone erosion and preserved the architecture of arthritic joints, and the study provides evidence that the cartilage protection of the OPG gene therapy may be associated with the down-regulation of MMP3 expression.
本研究检测了骨保护素(OPG)基因转移对小鼠胶原诱导性关节炎模型的影响。在患有关节炎的爪子上进行一次关节周围注射腺相关病毒载体-OPG(AAV-OPG)或腺相关病毒载体-乳糖酶基因(AAV-LacZ),成功地将外源基因整合到局部组织中,并在关节匀浆中导致显著的转基因表达,持续至少三周。从治疗后28天开始,接受OPG治疗的小鼠临床疾病评分显著改善(P < 0.05)。组织学评估表明,与LacZ对照组相比,OPG基因转移显著保护小鼠免受侵蚀性关节改变(P < 0.05),尽管治疗对局部炎症进展的效果似乎较差。显微CT数据表明,接受OPG治疗的胶原诱导性关节炎(CIA)小鼠的软骨下骨矿物质密度变化得到显著保护。有趣的是,OPG基因转移后,干扰素-γ(IFN-γ)和基质金属蛋白酶3(MMP3)的mRNA表达明显降低。总体而言,OPG基因转移有效抑制了关节炎相关的关节周围骨侵蚀,并保留了关节炎关节的结构,该研究提供了证据表明OPG基因治疗的软骨保护作用可能与MMP3表达的下调有关。